Phenomics & Genomics
We offer a range of services in next-generation sequencing technology and bioinformatics opening up a new dimension for integrating phenomics, molecular biology, and systems biology for mouse and human.
About
Next-generation sequencing technology and bioinformatics have opened up a new dimension for integrating phenomics, molecular biology, and systems biology for mouse and human. Our highly validated pipeline will accurately identify your variants using the following services.
Services
The APF team specializes in helping you to translate large, unwieldy sequencing datasets into manageable information in days, not months.
The Australian Phenome Bank handles all ordering requests. Please visit the Australian Phenome Bank website for further information.
The Australian Phenomics Facility experienced team of genomic and bioinformatic specialists offer exome and whole genome service packages built around researcher “end-to-end” requirements and provide a number of tools not otherwise available in a standard sequencing service.
BRF Illumina NGS technologies support a wide range of genomic applications, such as whole genome & exome sequencing, RNA-seq, epigenetics, metagenomics, HiC and more.
In vitro fertilisation (IVF) is used to re-animate strains from the frozen state from sources such as the repository of the Australian Phenome Bank. The team is using the latest and most efficient IVF techniques and re-animation success is currently running at 97% of attempts with sperm thawed from the APB archive.
We provide space, equipment and expertise to run small or large projects to map the chromosomal location and identify the affected gene of new gene-variant mouse strains obtained from N-ethyl-N-nitrosourea (ENU) libraries, spontaneous mutations or causative polymorphisms.
A certified Oxford Nanopore sequencing facility, delivering sample QC, library preparation and long-read seequencing solutions to the ANU, to Australia, and to overseas projects with MinION and PromethION technology.
The PacBio Revio, a cutting-edge DNA sequencer, accelerates research and drives innovation across various sectors.
We provide space, equipment and expertise to run small or large projects to map the chromosomal location and identify the affected gene of new gene-variant mouse strains obtained from N-ethyl-N-nitrosourea (ENU) libraries, spontaneous mutations or causative polymorphisms.
Depending on their housing and transportation conditions mouse strains may be carrying a multitude of pathogens that may or may not result in disease but may very well affect your experimental result outcomes.
We are committed to provide an excellent service, accurate results, fast turnaround times, at low cost.
We validate any SNVs identified through exome, whole genome or targeted sequencing.